BDBM50022454 3',4'-dihydro-2'H-spiro[imidazolidine-4,1'-naphthalene]-2,5-dione::3',4'-dihydro-2H,2'H,5H-spiro[imidazolidine-4,1'-naphthalene]-2,5-dione::CHEMBL289046::spiro[tetrahydro-1H-imidazole-4,1'-(1',2',3',4'-tetrahydronaphthalene)]-2,5-dione

SMILES O=C1NC(=O)C2(CCCc3ccccc23)N1

InChI Key InChIKey=OZYWLMZRNIFQPM-UHFFFAOYSA-N

Data  5 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50022454   

LigandPNGBDBM50022454(spiro[tetrahydro-1H-imidazole-4,1'-(1',2',3',4'-te...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of partially purified calf lens aldose reductase; value ranges from 10E-4 to 10e-5 MMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium channel protein type 1/2/3 subunit alpha(Rat)
University of Alabama At Birmingham

Curated by ChEMBL
LigandPNGBDBM50022454(spiro[tetrahydro-1H-imidazole-4,1'-(1',2',3',4'-te...)
Affinity DataIC50: 8.51E+5nMAssay Description:Inhibition of [3H]BTX-B binding to Neuronal voltage-dependent sodium channel of rat cerebral cortex synaptoneurosomesMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSodium channel protein type 1/2/3 subunit alpha(Rat)
University of Alabama At Birmingham

Curated by ChEMBL
LigandPNGBDBM50022454(spiro[tetrahydro-1H-imidazole-4,1'-(1',2',3',4'-te...)
Affinity DataIC50: 8.51E+5nMAssay Description:In vitro inhibition of Voltage-gated sodium channel by the displacement of [3H]batrachotoxin A 20-alpha-benzoate in rat brain cerebral cortex synapto...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAldo-keto reductase family 1 member B1(Human)
Kyushu University

Curated by ChEMBL
LigandPNGBDBM50022454(spiro[tetrahydro-1H-imidazole-4,1'-(1',2',3',4'-te...)
Affinity DataIC50: 8.01E+4nMAssay Description:Inhibition of human recombinant AKR1B1 assessed as D,L-glyceraldehyde reduction incubated in sodium phosphate buffer at pH 6.2 in presence of NADPHMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAldo-keto reductase family 1 member B1(Human)
Kyushu University

Curated by ChEMBL
LigandPNGBDBM50022454(spiro[tetrahydro-1H-imidazole-4,1'-(1',2',3',4'-te...)
Affinity DataIC50: 1.14E+5nMAssay Description:Aggregation-based inhibition of human recombinant AKR1B1 assessed as D,L-glyceraldehyde reduction incubated in sodium phosphate buffer at pH 6.2 in p...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed